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Midodrine HCl
Midodrine HCl - 21695-181-00 - (Midodrine Hydrochloride)
Drug Information of Midodrine HCl
| Product NDC: | 21695-181 |
| Proprietary Name: | Midodrine HCl |
| Non Proprietary Name: | Midodrine Hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; Midodrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Midodrine HCl
| Product NDC: | 21695-181 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076514 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020702 |
Package Information of Midodrine HCl
| Package NDC: | 21695-181-00 |
| Package Description: | 100 TABLET in 1 BOTTLE (21695-181-00) |
NDC Information of Midodrine HCl
| NDC Code | 21695-181-00 |
| Proprietary Name | Midodrine HCl |
| Package Description | 100 TABLET in 1 BOTTLE (21695-181-00) |
| Product NDC | 21695-181 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Midodrine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20020702 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | MIDODRINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC] |
